2-Chloro-5-iodopyridine

Names

[ Name ]:
2-Chloro-5-iodopyridine

[Synonym ]:
2-chloro-5-iodopyridine 2g
2-chloro-5-iodo pyridine
2-CHORO-5-IODOPYRIDINE
6-chloro-3-pyridinyl iodide
5-BroMo-5-iodopyridine
3-iodo-6-chloropyridine
5-iodo-2-chloropyridine
MFCD01863635
2-CHLORO-5-INDOPYRIDINE
2-Chlor-5-iodpyridin
4-chloro-1-iodopyridine

Biological Activity

[Description]:

2-Chloro-5-iodopyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
2.1±0.1 g/cm3

[ Boiling Point ]:
253.2±20.0 °C at 760 mmHg

[ Melting Point ]:
95-98 °C(lit.)

[ Molecular Formula ]:
C₅H₃ClIN

[ Molecular Weight ]:
239.44

[ Flash Point ]:
106.9±21.8 °C

[ Exact Mass ]:
238.899857

[ PSA ]:
12.89000

[ LogP ]:
2.40

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.642

[ Water Solubility ]:
insoluble

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R20/22;R36/37/38

[ Safety Phrases ]:
S26-S36-S36/37/39-S22

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

A short and efficient total synthesis of (±)-epibatidine.
A short and efficient total synthesis of (±)-epibatidine. Zhang C and Trudell ML.

J. Org. Chem. 61(20) , 7189-7191, (1996)

Synthesis of 5-Substituted 2,2'-Bipyridines from Substituted 2-Chloropyridines by a Modified Negishi Cross-Coupling Reaction. Lützen A and Hapke M.

European J. Org. Chem. 2002(14) , 2292-2297, (2002)

Synthesis of epibatidine isomers: Reductive Heck coupling of 2-azabicyclo [2.2.1] hept-5-ene derivatives. Cox CD and Malpass JR

Tetrahedron 55(40) , 11879-11888, (1999)